Evidence map›Paper›PMID 10024563›Full record

ArticleInfection and immunity1999

Isolation and chemical characterization of a capsular polysaccharide antigen shared by clinical isolates of Enterococcus faecalis and vancomycin-resistant Enterococcus faecium.

J Huebner, Y Wang, W A Krueger, L C Madoff, G Martirosian, S Boisot, D A Goldmann, D L Kasper, A O Tzianabos, G B Pier

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 139 citations in OpenAlex.

  1. Article
  2. Article
  3. Microbiology and molecular biology reviews : MMBR · 2024
    Review
  4. Article
  5. Enterococcal Membrane Vesicles as Vaccine Candidates.International journal of molecular sciences · 2023
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Pathogenicity of Enterococci.Microbiology spectrum · 2019
    Review
  15. Article
  16. Article
  17. Review
  18. Streamlined Synthesis and Evaluation of Teichoic Acid Fragments.Chemistry (Weinheim an der Bergstrasse, Germany) · 2018
    Article
  19. Article
  20. Prevalence and Genetic Diversity ofFrontiers in microbiology · 2017
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

J HuebnerChanning Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115-5899, USA.
Y Wang
W A Krueger
L C Madoff
G Martirosian
S Boisot
D A Goldmann
D L Kasper
A O Tzianabos
G B Pier
Brigham and Women's Hospital · USHarvard University · US

Funding

GROUP B STREPTOCOCCAL SURFACE PROTEINS IN IMMUNE EVASIONR01AI038424 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI MADOFF, LAWRENCE C. · 1997 to 2005
$1.5M
IMMUNOCHEMISTRY OF GROUP B STREPTOCOCCAL POLYSACCHARIDESR37AI023339 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KASPER, DENNIS L. · 1992 to 2001
$841k
Nutrient Sensing and Hexokinases in T. bruceiR15AI075326 · NIAID · CLEMSON UNIVERSITY · PI MORRIS, JAMES CULVIN · 2008 to 2012
$585k
Group B Streptococcal Surface Proteins in Immune EvasionR56AI038424 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI MADOFF, LAWRENCE C. · 2006 to 2006
$302k
ADHESINS OF COAGULASE-NEGATIVE STAPHYLOCOCCIR01AI023335 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI PIER, GERALD B · 1987 to 1999
–
GROUP B STREPTOCOCCAL SURFACE PROTEINS IN IMMUNE EVASIONR21AI038424 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI MADOFF, LAWRENCE C. · 1996 to 1996
–
IMMUNOCHEMISTRY OF GROUP B STREPTOCOCCAL POLYSACCHARIDESR01AI023339 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KASPER, DENNIS L. · 1985 to 1991
–
NIAID NIH HHS AI 23335NIAID NIH HHS AI23339NIAID NIH HHS AI 38424NIAID NIH HHS R01 AI038424NIAID NIH HHS R15 AI075326NIAID NIH HHS R56 AI038424
6 · The paper itself

Abstract

Enterococci are a common cause of serious infections, especially in newborns, severely immunocompromised patients, and patients requiring intensive care. To characterize enterococcal surface antigens that are targets of opsonic antibodies, rabbits were immunized with various gentamicin-killed Enterococcus faecalis strains, and immune sera were tested in an opsonophagocytic assay against a selection of clinical isolates. Serum raised against one strain killed the homologous strain (12030) at a dilution of 1:5,120 and mediated opsonic killing of 33% of all strains tested. In addition, this serum killed two (28%) of seven vancomycin-resistant Enterococcus faecium strains. Adsorption of sera with the homologous strain eliminated killing activity. The adsorbing antigens were resistant to treatment with proteinase K and to boiling for 1 h, but were susceptible to treatment with sodium periodate, indicating that the antigen inducing opsonic activity is a polysaccharide. Antibodies in immune rabbit sera reacted with a capsule-like structure visualized by electron microscopy both on the homologous E. faecalis strain and on a vancomycin-resistant E. faecium strain. The capsular polysaccharides from E. faecalis 12030 and E. faecium 838970 were purified, and chemical and structural analyses indicated they were identical glycerol teichoic acid-like molecules with a carbohydrate backbone structure of 6-alpha-D-glucose-1-2 glycerol-3-PO4 with substitution on carbon 2 of the glucose with an alpha-2-1-D-glucose residue. The purified antigen adsorbed opsonic killing activity from immune rabbit sera and elicited high titers of antibodies (when used to immunize rabbits) that both mediated opsonic killing of bacteria and bound to a capsule-like structure visualized by electron microscopy. These results indicate that approximately one-third of a sample of 15 E. faecalis strains and 7 vancomycin-resistant E. faecium strains possess shared capsular polysaccharides that are targets of opsonophagocytic antibodies and therefore are potential vaccine candidates.

Indexed as

AnimalsAntigens, BacterialBacterial CapsulesDrug Resistance, MicrobialEnterococcus faecalisEnterococcus faeciumHumansImmune SeraPolysaccharides, BacterialRabbitsVancomycinAntigens, BacterialImmune SeraPolysaccharides, BacterialVancomycin

Identifiers

PMID10024563
PMCPMC96449
OpenAlexW1902764168

What OpenQuestion holds

Texttitle and abstract
measurements read2
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.